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13877-55-9

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13877-55-9 Usage

General Description

7H-PYRAZOLO[4,3-D]PYRIMIDIN-7-ONE, 1,4-DIHYDRO- is a chemical compound that belongs to the class of pyrazolopyrimidine derivatives. It is a heterocyclic organic compound with a molecular formula of C7H8N4O. 7H-PYRAZOLO[4,3-D]PYRIMIDIN-7-ONE, 1,4-DIHYDRO- is a potent inhibitor of the enzyme dihydroorotate dehydrogenase (DHODH) and has shown potential as an antiviral and anticancer agent. Its structure and properties make it a promising candidate for further research and development in the fields of medicinal chemistry and drug discovery.

Check Digit Verification of cas no

The CAS Registry Mumber 13877-55-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,8,7 and 7 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 13877-55:
(7*1)+(6*3)+(5*8)+(4*7)+(3*7)+(2*5)+(1*5)=129
129 % 10 = 9
So 13877-55-9 is a valid CAS Registry Number.
InChI:InChI=1/C5H2N4O/c10-5-4-3(1-8-9-4)6-2-7-5/h1-2H

13877-55-9SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 7-Hydroxypyrazolo[4,3-d]pyrimidine

1.2 Other means of identification

Product number -
Other names 7H-PYRAZOLO[4,3-D]PYRIMIDIN-7-ONE, 1,4-DIHYDRO-

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:13877-55-9 SDS

13877-55-9Relevant articles and documents

Pyrazolo pyrimidines useful as aurora kinase inhibitors

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Page/Page column 84-85, (2010/11/25)

The present invention provides compounds having the formula: wherein A-B together represent one of the following structures: wherein one of is a double bond, as valency permits; and R2, R4, X1A, X2A, X1B, X2B, L1, L2, Y and Z are as defined in classes and subclasses herein, and pharmaceutical compositions thereof, as described generally and in subclasses herein, which compounds are useful as inhibitors of protein kinase (e.g., Aurora), and thus are useful, for example, for the treatment of Aurora mediated diseases.

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